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Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients
- Correspondence to: Dr F Moreno, Unidad de Genética Molecular, Hospital Ramón y Cajal, Carretera de Colmenar, Km 9, 28034 Madrid, Spain; fmoreno.hrc{at}salud.madrid.org
Citation
Uniparental disomy of chromosome 13q causing homozygosity for the 35delG mutation in the gene encoding connexin26 (GJB2) results in prelingual hearing impairment in two unrelated Spanish patients
Publication history
- First published August 14, 2003.
Online issue publication
April 27, 2016
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Copyright 2003 Journal of Medical Genetics